Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4783244
rs4783244
3 0.925 0.120 16 82628663 intron variant G/T snv 0.38 0.800 1.000 3 2011 2014
dbSNP: rs12051272
rs12051272
3 0.925 0.120 16 82629683 intron variant G/C;T snv 0.800 1.000 2 2012 2012
dbSNP: rs12597537
rs12597537
1 16 82637031 intron variant A/G snv 8.1E-02 0.700 1.000 1 2010 2010
dbSNP: rs12599599
rs12599599
1 16 82636934 intron variant G/A snv 3.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs16957913
rs16957913
1 16 82636644 intron variant T/C snv 3.7E-02 0.700 1.000 1 2010 2010
dbSNP: rs6565051
rs6565051
1 16 82625123 upstream gene variant G/A snv 0.72 0.700 1.000 1 2010 2010
dbSNP: rs7204454
rs7204454
1 16 82625589 upstream gene variant G/C snv 0.59 0.700 1.000 1 2010 2010